Gene: PDE4DIP (phosphodiesterase 4D interacting protein)  Homo sapiens
Symbol: PDE4DIP
Name: phosphodiesterase 4D interacting protein
Description: The protein encoded by this gene serves to anchor phosphodiesterase 4D to the Golgi/centrosome region of the cell. Defects in this gene may be a cause of myeloproliferative disorder (MBD) associated with eosinophilia. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2010]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: cardiomyopathy associated 2; cardiomyopathy-associated protein 2; CMYA2; DKFZp781J054; MGC75440; MMGL; myomegalin; OTTHUMP00000015720; OTTHUMP00000015721; OTTHUMP00000015722; OTTHUMP00000015723; OTTHUMP00000015724; OTTHUMP00000015725; OTTHUMP00000015726; OTTHUMP00000015727; OTTHUMP00000230044; OTTHUMP00000230074; OTTHUMP00000230075; OTTHUMP00000230076; OTTHUMP00000230091; OTTHUMP00000230125; OTTHUMP00000230506; phosphodiesterase 4D-interacting protein
Orthologs: Mus musculus : Pde4dip (phosphodiesterase 4D interacting protein (myomegalin))  MGI
Rattus norvegicus : Pde4dip (phosphodiesterase 4D interacting protein)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_11146,055,001 - 146,279,637-NCBI
Human Genome Assembly HuRef1119,142,103 - 119,150,668-NCBI
Human Genome Assembly HuRef1119,290,177 - 119,290,733-NCBI
Human Genome Assembly HuRef1119,268,039 - 119,268,441-NCBI
Human Genome Assembly HuRef1119,235,190 - 119,235,681-NCBI
Human Genome Assembly HuRef1119,196,278 - 119,206,459-NCBI
Human Genome Assembly HuRef1119,165,611 - 119,191,824-ENTREZGENE
Human Genome Assembly HuRef1119,153,321 - 119,162,328-NCBI
Human Genome Assembly GRCh371144,851,424 - 145,076,186-NCBI
Human Celera Assembly1121,506,245 - 121,526,690+NCBI
Human Genome Assembly Build 361143,562,784 - 143,787,436-NCBI
Human Cytogenetic Map1q12 NCBI
Human Genome Assembly1142,440,804 - 142,565,067 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)

Annotation    (Toggle Detail/Summary View)

Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
  
More on PDE4DIP
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 1352019
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2013-03-06
Status: ACTIVE



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